# K932429: Cordis Gravity Compensating Accessory

- Pathway: 510(k) (Traditional)
- Applicant: Cordis Corp.
- Decided: Jul 20, 1994 after 426 days
- Product code: JXG (Shunt, Central Nervous System And Components)
- Device class: 2
- Regulation: 21 CFR 882.5550
- Recalls of this device: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
4 later devices descend from it; 2 cite it directly.
0 of 5 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA has not posted a summary or statement for it, so its predicates are not known.

## Most influential descendants
- K020728: Miethke Shunt System (2002), 2 descendants of its own
- K242003: XABO Ventricular Catheter, XABO Peritoneal Catheter, XABO Catheter Set (2024), 0 descendants of its own
- K200950: Ventricular Catheter (2020), 0 descendants of its own
- K152897: Integra DP Valve Systems (including Burr Hole Reservoirs and Stainless Steel Connectors), Gravity Compensating Accessory (2016), 0 descendants of its own

## Recalls of this device
- Oct 3, 2008 · Not classified · Z-0458-2009: Integra NeuroSciences has become aware that certain Gravity Compensating Accessory implants have the potential for CSF leakage under certain conditions.

Source page: https://510kreport.com/device/K932429
Methodology: https://510kreport.com/methodology